Canonical Allele Identifier: CA354143923
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993656T>A , CM000665.2:g.121993656T>A GRCh38
NC_000003.11:g.121712503T>A , CM000665.1:g.121712503T>A GRCh37
NC_000003.10:g.123195193T>A NCBI36
NG_031870.1:g.33625A>T
NG_031870.2:g.71899A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1093A>T MANE Select ENSP00000345667.5:p.Arg365Trp
ENST00000460554.2:n.1043A>T
ENST00000642615.1:c.*276A>T ENSP00000495499.1:n.*276A>T
ENST00000273691.7:c.961A>T ENSP00000273691.3:p.Arg321Trp
ENST00000344209.9:c.1093A>T ENSP00000345667.5:p.Arg365Trp
ENST00000393631.5:c.826A>T ENSP00000377251.1:p.Arg276Trp
ENST00000460554.1:n.1195A>T
ENST00000462014.1:c.997A>T ENSP00000419414.1:p.Arg333Trp
NM_001199799.1:c.1093A>T NP_001186728.1:p.Arg365Trp
NM_001199800.1:c.826A>T NP_001186729.1:p.Arg276Trp
NM_175924.3:c.961A>T NP_787120.1:p.Arg321Trp
XM_005247389.3:c.997A>T XP_005247446.1:p.Arg333Trp
XM_011512738.1:c.1093A>T XP_011511040.1:p.Arg365Trp
XM_011512739.1:c.556A>T XP_011511041.1:p.Arg186Trp
XM_005247389.4:c.997A>T XP_005247446.1:p.Arg333Trp
XM_011512738.2:c.1093A>T XP_011511040.1:p.Arg365Trp
XM_011512739.2:c.556A>T XP_011511041.1:p.Arg186Trp
NM_001199799.2:c.1093A>T MANE Select NP_001186728.1:p.Arg365Trp
NM_001199800.2:c.826A>T NP_001186729.1:p.Arg276Trp
NM_175924.4:c.961A>T NP_787120.1:p.Arg321Trp